Primers used to amplify these regions prior to cloning were flanked with XbaI and XhoI or XhoI/SalI and SphI restriction enzyme sites (Table 3). Following digestion with the appropriate enzymes, the pair of PCR products was cloned into XbaI- and SphI-digested pUC19 in a three-way ligation, resulting in recombinant yitA or yipA sequence in which the stop codon was replaced by a 12-nt sequence containing XhoI and SalI restriction

sites. The mature domain of TEM-1 β-lactamase (lacking the N-terminal signal sequence that directs β-lactamase to selleck chemical the periplasm but including the stop codon) was amplified from pBR322 using primers flanked with XhoI and SalI sites. This fragment was then inserted into both recombinant pUC19 plasmids, resulting in plasmids that contained translational fusions of the YitA or YipA termini with β-lactamase, linked by the 6-nt XhoI sequence (introducing the 2 additional amino acids Leu and Glu) and flanked by 500 nt of

yitA or yipA downstream sequence following the β-lactamase stop codon. These constructs were digested from pUC19 using XbaI and SphI, gel purified, and ligated into the suicide cAMP vector pDS132 [30]. Selleckchem GSK1904529A Recombinant pDS132 plasmids containing yitA- or yipA-β-lactamase were placed into Escherichia coli S17-1 and transferred from E. coli S17-1 to Y. pestis via conjugation. Transconjugants were BKM120 ic50 selected

on Yersinia selective agar [31] with chloramphenicol, and verified by PCR. After overnight growth in brain heart infusion (BHI) broth without selection, transconjugants were placed on BHI agar containing 5% sucrose to select for allelic exchange mutants [32], which were further screened for chloramphenicol sensitivity and verified by PCR and Western blot analysis using anti-YitA, anti-YipA, and anti-β-lactamase antibodies (Millipore, Billerica, MA). Y. pestis was grown in BHI broth at 22°C overnight from frozen stocks and subcultured into fresh BHI at 22°C twice prior to each assay. Where appropriate, kanamycin (30 μg/mL), carbenicillin (100 μg/mL), or chloramphenicol (10 μg/mL) were added to the broth cultures at the indicated final concentration. Table 2 Y.